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Usher Syndrome

Audiology research (Pavia, Italy), 2022-01, Vol.12 (1), p.42-65

2022

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Similarities and Differences in Health, Social Trust, and Financial Situation in People With Usher Syndrome, a Bio-Psychosocial Perspective

Frontiers in psychology, 2020-08, Vol.11, p.1760-1760

2020

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Physical functioning in older persons with dizziness: a population-based study

Aging clinical and experimental research, 2017-04, Vol.29 (2), p.197-205

2017

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The ICF Core Sets for hearing loss: researcher perspective, Part II: Linking outcome measures to the International Classification of Functioning, Disability and Health (ICF)

International journal of audiology, 2014-02, Vol.53 (2), p.77-87

2014

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Life strategies of people with deafblindness due to Usher syndrome type 2a - a qualitative study

International journal of qualitative studies on health and well-being, 2019-01, Vol.14 (1), p.1656790

2019

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Functional validation of ABHD12 mutations in the neurodegenerative disease PHARC

Neurobiology of disease, 2017-02, Vol.98, p.36-51

2017

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The high prevalence of otitis media with effusion in children with cleft lip and palate as compared to children without clefts

International journal of pediatric otorhinolaryngology, 2009-10, Vol.73 (10), p.1441-1446

2009

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A combination of two truncating mutations in USH2A causes more severe and progressive hearing impairment in Usher syndrome type IIa

Hearing research, 2016-09, Vol.339, p.60-68

2016

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A longitudinal study of hearing and middle ear status in adolescents with cleft lip and palate

The Laryngoscope, 2013-06, Vol.123 (6), p.1374-1380

2013

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The creation of a comprehensive and a brief core set for hearing loss using the international classification of functioning, disability and health

American journal of audiology, 2013-12, Vol.22 (2), p.323-328

2013

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The ICF Core Sets for hearing loss - researcher perspective. Part I: Systematic review of outcome measures identified in audiological research

International journal of audiology, 2014-02, Vol.53 (2), p.65-76

2014

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Headphone listening habits and hearing thresholds in swedish adolescents

Noise & health, 2017-05, Vol.19 (88), p.125-132

2017

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The lived experiences of work and health of people living with deaf-blindness due to Usher syndrome type 2

International journal of qualitative studies on health and well-being, 2020-01, Vol.15 (1), p.1846671-1846671

2020

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Otosclerosis: Thirty-Year Follow-Up After Surgery

Annals of otology, rhinology & laryngology, 2011-09, Vol.120 (9), p.608-614

2011

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Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment

American journal of medical genetics. Part A, 2011-06, Vol.155A (6), p.1298-1313

2011

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Outcome of primary treatment of early laryngeal malignancies using photodynamic therapy

Acta oto-laryngologica, 2014-08, Vol.134 (8), p.852-858

2014

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Health, work, social trust, and financial situation in persons with Usher syndrome type 1

Work (Reading, Mass.), 2018-01, Vol.60 (2), p.209-220

2018

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Implications of Deafblindness: The Physical and Mental Health and Social Trust of Persons with Usher Syndrome Type 3

Journal of visual impairment & blindness, 2016-07, Vol.110 (4), p.245-256

2016

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Headphone listening habits, hearing thresholds and listening levels in Swedish adolescents with severe to profound HL and adolescents with normal hearing

International journal of audiology, 2018-10, Vol.57 (10), p.730-736

2018

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Hearing-related, health-related quality of life in patients who have undergone otosclerosis surgery: A long-term follow-up study

International journal of audiology, 2015-02, Vol.54 (2), p.63-69

2015

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The Relationship between Work and Health in Persons with Usher Syndrome Type 2

Journal of visual impairment & blindness, 2016-07, Vol.110 (4), p.233-244

2016

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Cognitive skills in children with Usher syndrome type 1 and cochlear implants

International journal of pediatric otorhinolaryngology, 2012-10, Vol.76 (10), p.1449-1457

2012

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Oral therapy for riboflavin transporter deficiency - What is the regimen of choice?

Parkinsonism & related disorders, 2019-04, Vol.61, p.245-247

2019

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Physical and Psychological Health in Persons with Deafblindness that is due to Usher Syndrome Type II

Journal of visual impairment & blindness, 2013-05, Vol.107 (3), p.207-220

2013

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Usher Syndrome

Similarities and Differences in Health, Social Trust, and Financial Situation in People With Usher Syndrome, a Bio-Psychosocial Perspective

Physical functioning in older persons with dizziness: a population-based study

The ICF Core Sets for hearing loss: researcher perspective, Part II: Linking outcome measures to the International Classification of Functioning, Disability and Health (ICF)

Life strategies of people with deafblindness due to Usher syndrome type 2a - a qualitative study

Functional validation of ABHD12 mutations in the neurodegenerative disease PHARC

The high prevalence of otitis media with effusion in children with cleft lip and palate as compared to children without clefts

A combination of two truncating mutations in USH2A causes more severe and progressive hearing impairment in Usher syndrome type IIa

A longitudinal study of hearing and middle ear status in adolescents with cleft lip and palate

The creation of a comprehensive and a brief core set for hearing loss using the international classification of functioning, disability and health

The ICF Core Sets for hearing loss - researcher perspective. Part I: Systematic review of outcome measures identified in audiological research

Headphone listening habits and hearing thresholds in swedish adolescents

The lived experiences of work and health of people living with deaf-blindness due to Usher syndrome type 2

Otosclerosis: Thirty-Year Follow-Up After Surgery

Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment

Outcome of primary treatment of early laryngeal malignancies using photodynamic therapy

Health, work, social trust, and financial situation in persons with Usher syndrome type 1

Implications of Deafblindness: The Physical and Mental Health and Social Trust of Persons with Usher Syndrome Type 3

Headphone listening habits, hearing thresholds and listening levels in Swedish adolescents with severe to profound HL and adolescents with normal hearing

Hearing-related, health-related quality of life in patients who have undergone otosclerosis surgery: A long-term follow-up study

The Relationship between Work and Health in Persons with Usher Syndrome Type 2

The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management

Cognitive skills in children with Usher syndrome type 1 and cochlear implants

Oral therapy for riboflavin transporter deficiency - What is the regimen of choice?

Physical and Psychological Health in Persons with Deafblindness that is due to Usher Syndrome Type II

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